Ashraf Wilsily
Affiliations: | 2012 | California Institute of Technology, Pasadena, CA |
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| Fillion E, Beaton E, Nguyen Y, et al. (2016) Facile Hydrogenolysis of C(sp3)-C(sp3) σ Bonds Advanced Synthesis & Catalysis. 358: 3422-3434 |
| Lundgren RJ, Wilsily A, Marion N, et al. (2013) Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoates. Angewandte Chemie (International Ed. in English). 52: 2525-8 |
| Wilsily A, Tramutola F, Owston NA, et al. (2012) New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles. Journal of the American Chemical Society. 134: 5794-7 |
| Fillion E, Lou T, Liao ET, et al. (2012) Catalytic intramolecular friedel-crafts reaction of benzyl meldrum's acid derivatives: Preparation of 5,6-dimethoxy-2-methyl-1-indanone Organic Syntheses. 89: 115-125 |
| Lu Z, Wilsily A, Fu GC. (2011) Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides. Journal of the American Chemical Society. 133: 8154-7 |
| Wilsily A, Fillion E. (2009) Asymmetric synthesis of all-carbon benzylic quaternary stereocenters via conjugate addition to alkylidene and indenylidene Meldrum's acids. The Journal of Organic Chemistry. 74: 8583-94 |
| Wilsily A, Nguyen Y, Fillion E. (2009) Hydrogenolysis of unstrained carbon-carbon sigma bonds: stereoselective entry into benzylic tertiary centers. Journal of the American Chemical Society. 131: 15606-7 |
| Fillion E, Wilsily A, Fishlock D. (2009) Probing persistent intramolecular C-H...X (X = O, S, Br, Cl, and F) bonding in solution using benzyl Meldrum's acid derivatives. The Journal of Organic Chemistry. 74: 1259-67 |
| Wilsily A, Lou T, Fillion E. (2009) Enantioselective copper-catalyzed conjugate addition of dimethylzinc to 5-(1-arylalkylidene) Meldrum's acids Synthesis. 2066-2072 |
| Wilsily A, Fillion E. (2008) Asymmetric synthesis of carboxylic acid derivatives having an all-carbon alpha-quaternary center through Cu-catalyzed 1,4-addition of dialkylzinc reagents to 2-aryl acetate derivatives. Organic Letters. 10: 2801-4 |